Trititanate‐nanosheet incorporated hydrogels: Self‐initiated photopolymerization and application in photodegradation of methylene violet
Source abstract
Abstract
Exposing the aqueous mixtures of acrylamide (AAm) monomers and exfoliated trititanate nanosheets (TiNs) to ultraviolet light achieved nanocomposite hydrogels TiNs–PAAm in a facile one‐step synthetic route. The incorporated semiconductor TiNs functioned as a photocatalytic crosslinker, initiating the in situ photopolymerization of monomers and hydrogen‐bonding crosslinking with the polymeric networks to form nanocomposite hydrogels. The resultant hydrogels exhibited good absorption behaviors of methylene violet (MV), and the hydrogel prepared from an AAm/TiNs ratio of 2.46 × 102 g/g exhibited a maximum uptake of 8.4 g MV solution for 1 g. The immobilized TiNs retained high photocatalytic activity in the recyclable photodegradation of MV. It indicated the nanocomposite hydrogels may be considered as a good candidate in wastewater treatment. POLYM. COMPOS., 37:2811–2819, 2016. © 2015 Society of Plastics Engineers
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Conducting polymers and applications · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Fujian Key Laboratory of Functional Materials, College of Materials Science and Engineering Huaqiao University Xiamen 361021 China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Fujian and the Province
References (41)
Show source-provided references
1. 10.1002/1097-4636(20000905)51:3<293::AID-JBM1>3.0.CO;2-T10.1002/1097-4636(20000905)51:3<293::AID-JBM1>3.0.CO;2-T ↗
2. 10.1016/j.ejpb.2007.02.01410.1016/j.ejpb.2007.02.014 ↗
3. 10.1039/c0sm00067a10.1039/c0sm00067a ↗
4. 10.1021/jp907974d10.1021/jp907974d ↗
5. 10.1007/s00289-006-0552-010.1007/s00289-006-0552-0 ↗
6. 10.1002/app.2906110.1002/app.29061 ↗
7. 10.1021/cr970028210.1021/cr9700282 ↗
8. 10.1146/annurev.bioeng.2.1.910.1146/annurev.bioeng.2.1.9 ↗
9. 10.1039/c1sm05890h10.1039/c1sm05890h ↗
10. 10.1039/b925218p10.1039/b925218p ↗
11. 10.1016/j.synthmet.2010.01.02410.1016/j.synthmet.2010.01.024 ↗
12. 10.1002/1521-4095(20020816)14:16<1120::AID-ADMA1120>3.0.CO;2-910.1002/1521-4095(20020816)14:16<1120::AID-ADMA1120>3.0.CO;2-9 ↗
13. 10.1007/s00396-013-3021-y10.1007/s00396-013-3021-y ↗
14. 10.1002/anie.20120026710.1002/anie.201200267 ↗
15. 10.1038/nature0869310.1038/nature08693 ↗
16. 10.1002/chem.20090014910.1002/chem.200900149 ↗
17. 10.1002/adma.20030651610.1002/adma.200306516 ↗
18. 10.1002/smll.20110206010.1002/smll.201102060 ↗
19. 10.1038/srep0139910.1038/srep01399 ↗
20. 10.1002/adma.20050269610.1002/adma.200502696 ↗
21. 10.1016/j.jhazmat.2014.07.06810.1016/j.jhazmat.2014.07.068 ↗
22. 10.1021/cr00033a00410.1021/cr00033a004 ↗
23. 10.1021/es980923i10.1021/es980923i ↗
24. 10.1002/adma.20100172210.1002/adma.201001722 ↗
25. 10.1038/ncomms302910.1038/ncomms3029 ↗
26. 10.1016/j.jphotochem.2005.10.02110.1016/j.jphotochem.2005.10.021 ↗
27. 10.1021/ma070798810.1021/ma0707988 ↗
28. 10.1007/s00396-004-1257-210.1007/s00396-004-1257-2 ↗
29. 10.1021/j100239a01210.1021/j100239a012 ↗
30. 10.1021/ja202760x10.1021/ja202760x ↗
31. Bryant S.J. · Biomed. Sci. Instrum. · 1998 · 35 · 309
32. 10.1002/jbm.a.3213410.1002/jbm.a.32134 ↗
33. 10.1039/b921692h10.1039/b921692h ↗
34. 10.1016/j.electacta.2012.07.08510.1016/j.electacta.2012.07.085 ↗
35. 10.1016/S1010-6030(99)00199-910.1016/S1010-6030(99)00199-9 ↗
36. 10.1021/j100534a01210.1021/j100534a012 ↗
37. 10.1021/jo00110a04210.1021/jo00110a042 ↗
38. 10.1070/MC1995v005n03ABEH00047710.1070/MC1995v005n03ABEH000477 ↗
39. 10.1016/0957-4166(96)00195-410.1016/0957-4166(96)00195-4 ↗
40. 10.1002/jps.260066101110.1002/jps.2600661011 ↗
41. 10.3109/0049825780906958510.3109/00498257809069585 ↗